Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation - Full text - MIT Libraries
F Zhao, CG Weismann, M Satoda, ME Pierpont, E … - Am J Hum Genet, 2001 - journals.uchicago.edu
... International Agency for Research on Cancer TP53 Mutation Database, http://www.iarc ...
MIM 169100], TFAP2A [MIM 107580], TFAP2B [MIM 601601], and TFAP2C [MIM 601602 ...
Cited by 13 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

ERTargetDB: an integral information resource of transcription regulation of ER target genes
VX Jin, H Sun, TT Pohar, S Liyanarachchi, SK … - journals.endocrinology.org
... 26 TFAP2C 1 Hs.473152 120 134 tGGTCAccgTGACCc 27 TFAP2C 2 Hs.473152 68 82
cgtgtccagTGACCc 27 TFF1 Hs.162807 112 126 aGGTCAcggTGGCCa 28 ...
View as HTML - Web Search

Relevance of Breast Cancer Cell Lines as Models for Breast Tumours: An Update - Full text - MIT Libraries
M Lacroix, G Leclercq - Breast Cancer Research and Treatment, 2004 - springerlink.com
... HCC1937 BCC also have an acquired mutation of TP53 with wild-allele loss,
and an acquired homozygous deletion of the PTEN gene. ...
Cited by 16 - Web Search - kluweronline.com - geocities.com - ncbi.nlm.nih.gov - all 5 versions »